6,993 research outputs found

    Status of Marine Birds of the Southeastern Beaufort Sea

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    This summary and update of information on the marine birds of the southeastern Beaufort Sea is intended to support discussions on how to improve management of marine resources in the Canadian Beaufort Sea region. Perhaps the most outstanding use of the Beaufort Sea by marine birds is the staging during spring migration by hundreds of thousands of eiders and long-tailed ducks in the early open water off Cape Bathurst and Banks Island. During midsummer, tens of thousands of long-tailed ducks, scoters, scaup, and mergansers moult in the sheltered bays and behind barrier beaches and spits. Although several species of geese, ducks, loons, gulls, and terns nest on islands and in wetlands along the Beaufort Sea coast, this region has relatively few nesting seabirds compared to eastern Arctic Canada and the Bering Sea. Two possible reasons for this are a shortage of cliffs suitable for nesting and a lack of pelagic fish. The five most common sea duck species that occur in the region, long-tailed duck, king eider, common eider, surf scoter, and white-winged scoter, have all declined in numbers since the mid-1970s. Western Arctic brant populations have also declined, although their status within the Beaufort Sea region is unclear. Brant and king eider are the only marine bird species harvested there in substantial numbers. Other threats to Beaufort Sea marine bird populations include oil spills, global warming, coastal development, and contaminants. Certain threats can be managed at a local level since they are a result of local economic development, but others, such as global warming or loss of critical wintering areas, stem from environmental problems outside the region. Solving these issues will require mutual understanding and commitment on the part of numerous countries.Cette récapitulation et mise à jour de l'information sur les oiseaux marins du sud-est de la mer de Beaufort ont été faites dans le but de fournir des arguments sur la façon d'améliorer la gestion des ressources marines dans la zone canadienne de la mer de Beaufort. L'utilisation la plus notable que font les oiseaux marins de la mer de Beaufort est peut-être en tant que halte durant la migration printanière de centaines de milliers d'eiders et de canards à longue queue dans les premières eaux libres au large du cap Bathurst et de l'île Banks. Au milieu de l'été, des dizaines de milliers de canards à longue queue, de macreuses, de fuligules milouinans et de harles muent dans les baies abritées et en arrière des flèches et cordons littoraux. Même si plusieurs espèces d'oies, de canards, de huarts, de mouettes et de sternes nichent sur les îles et dans les zones humides longeant le rivage de la mer de Beaufort, cette région voit relativement peu d'oiseaux marins qui viennent y nicher en comparaison de l'est du Canada arctique et de la mer de Béring. Il y a deux raisons possibles à cet état de choses: trop peu de falaises propices à l'établissement de nids et un manque de poissons pélagiques. Les cinq espèces de canards de mer les plus courantes dans la région, à savoir, le canard à longue queue, l'eider à tête grise, l'eider à duvet, la macreuse à front blanc et la macreuse brune, ont toutes vu leurs nombres décliner depuis le milieu des années 1970. La population de bernaches cravants de l'ouest de l'Arctique est également en déclin, bien que le statut de cet oiseau au sein de la région de la mer de Beaufort ne soit pas évident. La bernache cravant et l'eider à tête grise sont les seules espèces d'oiseaux marins prélevées en nombre important à cet endroit. Parmi les autres facteurs qui menacent les populations d'oiseaux marins de la mer de Beaufort, on compte les déversements d'hydrocarbures, le réchauffement climatique, l'aménagement du littoral et les contaminants. Certaines menaces peuvent être gérées au niveau local vu qu'elles résultent du développement économique local, mais d'autres comme le réchauffement climatique ou la perte d'aires d'hivernage critiques sont issues d'enjeux environnementaux extérieurs à la région. La résolution de ces problèmes passe obligatoirement par une compréhension et un engagement mutuels de la part de nombreux pays

    Algorithmic approach to adiabatic quantum optimization

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    It is believed that the presence of anticrossings with exponentially small gaps between the lowest two energy levels of the system Hamiltonian, can render adiabatic quantum optimization inefficient. Here, we present a simple adiabatic quantum algorithm designed to eliminate exponentially small gaps caused by anticrossings between eigenstates that correspond with the local and global minima of the problem Hamiltonian. In each iteration of the algorithm, information is gathered about the local minima that are reached after passing the anticrossing non-adiabatically. This information is then used to penalize pathways to the corresponding local minima, by adjusting the initial Hamiltonian. This is repeated for multiple clusters of local minima as needed. We generate 64-qubit random instances of the maximum independent set problem, skewed to be extremely hard, with between 10^5 and 10^6 highly-degenerate local minima. Using quantum Monte Carlo simulations, it is found that the algorithm can trivially solve all the instances in ~10 iterations.Comment: 7 pages, 3 figure

    Biologically Inspired Feedback Design for Drosophila Flight

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    We use a biologically motivated model of the Drosophila's flight mechanics and sensor processing to design a feedback control scheme to regulate forward flight. The model used for insect flight is the grand unified fly (GUF) [3] simulation consisting of rigid body kinematics, aerodynamic forces and moments, sensory systems, and a 3D environment model. We seek to design a control algorithm that will convert the sensory signals into proper wing beat commands to regulate forward flight. Modulating the wing beat frequency and mean stroke angle produces changes in the flight envelope. The sensory signals consist of estimates of rotational velocity from the haltere organs and translational velocity estimates from visual elementary motion detectors (EMD's) and matched retinal velocity filters. The controller is designed based on a longitudinal model of the flight dynamics. Feedforward commands are generated based on a desired forward velocity. The dynamics are linearized around this operating point and a feedback controller designed to correct deviations from the operating point. The control algorithm is implemented in the GUF simulator and achieves the desired tracking of the forward reference velocities and exhibits biologically realistic responses

    Two Types of Resistance to the Diamondback Moth (Lepidoptera: Plutellidae) in Cabbage

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    Survival of larvae of the diamondback moth, Plutella xylostella (L.) was reduced on several genotypes of cabbage from the breeding program at Geneva, N.Y. Polar fractions of ethanol extracts of partially resistant lines 2535 and 2503, when incorporated into diet, reduced survival of P. xylostella larvae by 14.9 and 19.0%, respectively. Whether this effect was due to reduced feeding or postingestive toxicity was not determined. Although survival on glossy-leafed line 2518 was very low in the field and larvae on this line failed to form visible feeding mines during the first 72 h after egg hatch, extracts from 2518 had no activity. Survival of larvae confined on leaf disks of 2518 in the laboratory was much greater (80% of controls) than it was on whole plants in the field (0.36% of controls). In the field, neonate P. xylostella dispersed two to three times more rapidly on the leaves of 2518 than on other lines. Resistance to P. xylostella in the lines investigated was therefore due to at least two mechanisms, (1) antibiosis or nonpreference due to extractable compounds present in normal bloom resistant cabbage genotypes, 2503 and 2535, and (2) possible nonpreference for glossy-leafed 2518 by neonate larvae, as suggested by the greater dispersal rates of neonates on these plants. Survival is relatively high on 2518 in leaf disk bioassays in the laboratory, suggesting that nonpreference in combination with environmental stresses to larvae in the field may produce P. xylostella resistance in the glossy 251

    Integrative Model of Drosophila Flight

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    This paper presents a framework for simulating the flight dynamics and control strategies of the fruit fly Drosophila melanogaster. The framework consists of five main components: an articulated rigid-body simulation, a model of the aerodynamic forces and moments, a sensory systems model, a control model, and an environment model. In the rigid-body simulation the fly is represented by a system of three rigid bodies connected by a pair of actuated ball joints. At each instant of the simulation, the aerodynamic forces and moments acting on the wings and body of the fly are calculated using an empirically derived quasi-steady model. The pattern of wing kinematics is based on data captured from high-speed video sequences. The forces and moments produced by the wings are modulated by deforming the base wing kinematics along certain characteristic actuation modes. Models of the fly’s visual and mechanosensory systems are used to generate inputs to a controller that sets the magnitude of each actuation mode, thus modulating the forces produced by the wings. This simulation framework provides a quantitative test bed for examining the possible control strategies employed by flying insects. Examples demonstrating pitch rate, velocity, altitude, and flight speed control, as well as visually guided centering in a corridor are presented

    Oyster Mortality Studies in Virginia: Ill. Epizootiology of a Disease Caused by Haplosporidium costale Wood and Andrews

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    A short, sharp eplzootic disease of oysters on Seaside of Eastern Shore, Virginia, has been associated with a new pathogen, Haplosporidium costale Wood and Andrews. Native oysters in trays have shown closely timed May-June losses for three consecutive years. Losses at other seasons were small. May-June losses ranged from 12 to 14 percent in 1959 to 36 to 44 percent in 1960. James River oysters moved to Seaside showed higher losses than natives after a year of acclimation. Oysters in Bayside creeks revealed late summer losses caused by Dermocystidimn marinmn Mackin, Owens, and Collier rather than May-June deaths. The new pathogen was found in live oysters from March to July, and in a high proportion of gapers in May and June. The epizootiology is well established for these periods but unknown for the rest of the year. Increasing prevalence of another pathogen ( MSX ), causing Delaware Bay disease, has complicated mortality studies. Losses are most serious in older oysters which have been held beyond the usual period of culture. Careful timing of planting and early harvesting permit oystermen to a void serious losses

    On Nichols algebras over PGL(2,q) and PSL(2,q)

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    We compute necessary conditions on Yetter-Drinfeld modules over the groups \mathbf{PGL}(2,q)=\mathbf{PGL}(2,\FF_q) and \mathbf{PSL}(2,q)=\mathbf{PSL}(2,\FF_q) to generate finite dimensional Nichols algebras. This is a first step towards a classification of pointed Hopf algebras with group of group-likes isomorphic to one of these groups. As a by-product of the techniques developed in this work, we prove that there is no non-trivial finite-dimensional pointed Hopf algebra over the Mathieu groups M20M_{20} and M21=PSL(3,4)M_{21}=\mathbf{PSL}(3,4).Comment: Minor change

    A nucleotide sequence from a ribonuclease III processing site in bacteriophage T7 RNA.

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    Immune-Mediated Inflammation May Contribute to the Pathogenesis of Cardiovascular Disease in Mucopolysaccharidosis Type I.

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    BackgroundCardiovascular disease, a progressive manifestation of α-L-iduronidase deficiency or mucopolysaccharidosis type I, continues in patients both untreated and treated with hematopoietic stem cell transplantation or intravenous enzyme replacement. Few studies have examined the effects of α-L-iduronidase deficiency and subsequent glycosaminoglycan storage upon arterial gene expression to understand the pathogenesis of cardiovascular disease.MethodsGene expression in carotid artery, ascending, and descending aortas from four non-tolerized, non-enzyme treated 19 month-old mucopolysaccharidosis type I dogs was compared with expression in corresponding vascular segments from three normal, age-matched dogs. Data were analyzed using R and whole genome network correlation analysis, a bias-free method of categorizing expression level and significance into discrete modules. Genes were further categorized based on module-trait relationships. Expression of clusterin, a protein implicated in other etiologies of cardiovascular disease, was assessed in canine and murine mucopolysaccharidosis type I aortas via Western blot and in situ immunohistochemistry.ResultsGene families with more than two-fold, significant increased expression involved lysosomal function, proteasome function, and immune regulation. Significantly downregulated genes were related to cellular adhesion, cytoskeletal elements, and calcium regulation. Clusterin gene overexpression (9-fold) and protein overexpression (1.3 to 1.62-fold) was confirmed and located specifically in arterial plaques of mucopolysaccharidosis-affected dogs and mice.ConclusionsOverexpression of lysosomal and proteasomal-related genes are expected responses to cellular stress induced by lysosomal storage in mucopolysaccharidosis type I. Upregulation of immunity-related genes implicates the potential involvement of glycosaminoglycan-induced inflammation in the pathogenesis of mucopolysaccharidosis-related arterial disease, for which clusterin represents a potential biomarker

    Open fissures along faults: Variscan examples from Gower, South Wales

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    The extent to which persistent, rather than transient, fissures (wide planar voids) can exist along upper crustal faults is important in assessing fault permeability to mineral and hydrocarbon-bearing fluids. Variscan (late Carboniferous) faults cutting Dinantian (Lower Carboniferous) limestones on the Gower peninsula, South Wales, host clear evidence for fissures up to several metres wide. Evidence includes dendritic hematite growth and elongate calcite growth into open voids, spar ball and cockade breccia formation, laminated sediment infill and void-collapse breccias. Detailed mapping reveals cross-cutting geometries and brecciation of earlier fissure fills, showing that fissures were formed during, rather than after, active faulting. Fissures therefore probably formed by geometric mismatch between displaced fault walls, rather than by solution widening along inactive faults
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